HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059158Generated: October 27, 2026
Dichloromethane → 17,21-Diacetoxy-6-methylene-4-pregnene-3,20-dione
https://huagongshe.com/reaction/2059158
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Reactant | 17,21-Bis(acetyloxy)pregn-4-ene-3,20-dione | HCID 102165 | — |
| Solvent | Dimethoxymethane | HCID 8020 | — |
| Product | 17,21-Diacetoxy-6-methylene-4-pregnene-3,20-dione | HCID 12951771 | — |
Reaction Steps
A solution of 5.0 g of 17,21-diacetoxy-4-pregnene-3,20-dione in 35 ml of anhydrous methylene chloride and 22.5 ml of methylal is combined in incremental portions at room temperature with a mixture of 1.0 g of phosphorus pentoxide and 7.5 g of silica gel. The mixture is agitated for 3 days at room temperature and then another 11 ml of methylal, 500 mg of phosphorus pentoxide, and 3.75 g of silica gel are added. After another 2 days, the reaction mixture is vacuum-filtered, the residue is washed thoroughly with methylene chloride, and evaporated to dryness under vacuum. The crude product is purified on 350 g of silica gel with a hexane/ethyl acetate gradient (0-50% ethyl acetate), thus obtaining 3.6 g of 17α,21-diacetoxy-6-methylene-4-pregnene-3,20-dione, mp 227°-228° C. [α]D25 =+165° (chloroform).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04322349 |
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| Source dataset | uspto-grants-1982_03 |
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| ORD ID | ord-4f9d0d0d87674fb89a42961937347e3b |
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| Source note | uspto-grants-1982_03 |
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